Journal of Microencapsulation · 1993 · 19 citations · 16 references
PharmacyPharmaceuticsControlled Release FormulationsDrug DeliveryPharmaceutical FormulationControlled Release MechanismsDrug EncapsulationDrug Release From Dosage FormsDrug Release KineticsControlled Release MicrospheresFirst-order Drug ReleaseHiguchi ModelKinetic Data AnalysisMicrosphere FormulationsMicrospheresRelease KineticsRelease Mechanism Analysis
Poly(l-lactic acid) microspheres containing oestrone were prepared by the solvent evaporation method using methylene chloride as the casting solvent and poly(vinyl alcohol) as the emulsifier. Non-agglomerated microspheres with average diameters of 125-160 microns, containing 3-18 per cent oestrone were prepared successfully using a stirring rate of 650 rpm and a poly(vinyl alcohol) concentration as low as 0.15%. Drug loading decreased with an increase in the relative amounts of methylene chloride or emulsifier. Microspheres with 9 per cent loading released approximately 50 per cent of the drug in the first 12 h and the remainder at a much slower rate over several days. Initial examination revealed that the kinetic data followed both a first-order release pattern and the Higuchi matrix model. Differential rate treatment confirmed the Higuchi matrix model and the release mechanism was determined to be diffusion-controlled.
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Philip L. Ritger, Nikolaos A. Peppas · Journal of Controlled Release · 1987 · 3.7K citations
Analysis of Fickian and non-Fickian drug release from polymers.
Nicholas A. Peppas · PubMed · 1985 · 2.1K citations